Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7766029 | 0.851 | 0.080 | 6 | 88137716 | downstream gene variant | T/C | snv | 0.51 | 7 | ||
rs10801153 | 0.925 | 0.080 | 1 | 192794818 | intron variant | G/A | snv | 0.27 | 3 | ||
rs2463107 | 1.000 | 0.040 | 12 | 79699537 | intron variant | A/C | snv | 0.36 | 2 | ||
rs2572431 | 1.000 | 0.040 | 8 | 11247568 | downstream gene variant | C/G;T | snv | 2 | |||
rs34548976 | 1.000 | 0.040 | 7 | 31032854 | intergenic variant | C/T | snv | 0.39 | 2 | ||
rs4813627 | 1.000 | 0.040 | 20 | 3074867 | downstream gene variant | A/G | snv | 0.51 | 2 | ||
rs11059336 | 12 | 127745489 | regulatory region variant | T/C | snv | 0.14 | 1 | ||||
rs113209956 | 9 | 25211195 | intergenic variant | C/T | snv | 5.4E-02 | 1 | ||||
rs1192553 | 1 | 17967858 | intergenic variant | G/A | snv | 0.70 | 1 | ||||
rs1458103 | 11 | 81336231 | intron variant | A/C | snv | 0.25 | 1 | ||||
rs72711240 | 4 | 134774652 | intron variant | C/T | snv | 2.2E-02 | 1 | ||||
rs9875578 | 3 | 13752941 | intergenic variant | G/A;C | snv | 1 | |||||
rs1922242 | 0.827 | 0.120 | 7 | 87544351 | intron variant | A/T | snv | 0.43 | 8 | ||
rs1202184 | 0.851 | 0.120 | 7 | 87584585 | intron variant | C/T | snv | 0.39 | 7 | ||
rs1401663578 | 0.882 | 0.120 | 17 | 63483037 | missense variant | A/G | snv | 1.4E-05 | 4 | ||
rs2451828 | 5 | 7448683 | intron variant | C/T | snv | 2.7E-02 | 1 | ||||
rs4822492 | 1.000 | 0.040 | 22 | 24447626 | intron variant | C/G | snv | 0.47 | 4 | ||
rs2298383 | 0.827 | 0.200 | 22 | 24429543 | non coding transcript exon variant | C/A;T | snv | 11 | |||
rs5751876 | 0.742 | 0.320 | 22 | 24441333 | synonymous variant | T/C | snv | 0.54 | 0.52 | 16 | |
rs3761422 | 1.000 | 0.040 | 22 | 24430704 | intron variant | T/C | snv | 0.62 | 4 | ||
rs3930965 | 1.000 | 0.040 | 10 | 4971951 | intron variant | G/A;C | snv | 2 | |||
rs900418273 | 0.807 | 0.120 | 11 | 113393764 | missense variant | A/G | snv | 8 | |||
rs63750264 | 0.716 | 0.360 | 21 | 25891784 | missense variant | C/A;G;T | snv | 17 | |||
rs63750579 | 0.742 | 0.280 | 21 | 25891856 | missense variant | C/G;T | snv | 13 | |||
rs2306073 | 0.882 | 0.080 | 12 | 27402904 | intron variant | C/T | snv | 0.37 | 4 |